JP2015529273A - 樹脂組成物及び樹脂を含有する複合構造体 - Google Patents
樹脂組成物及び樹脂を含有する複合構造体 Download PDFInfo
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- JP2015529273A JP2015529273A JP2015532470A JP2015532470A JP2015529273A JP 2015529273 A JP2015529273 A JP 2015529273A JP 2015532470 A JP2015532470 A JP 2015532470A JP 2015532470 A JP2015532470 A JP 2015532470A JP 2015529273 A JP2015529273 A JP 2015529273A
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- Prior art keywords
- fluorene
- bis
- aminophenyl
- resin
- epoxy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 229920005989 resin Polymers 0.000 title claims abstract description 85
- 239000011347 resin Substances 0.000 title claims abstract description 85
- 239000011342 resin composition Substances 0.000 title claims abstract description 16
- 239000000805 composite resin Substances 0.000 title 1
- 229920000647 polyepoxide Polymers 0.000 claims abstract description 100
- 239000003822 epoxy resin Substances 0.000 claims abstract description 90
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 claims abstract description 84
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 claims abstract description 32
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 31
- 239000002131 composite material Substances 0.000 claims abstract description 9
- FPRFOKKPDUHQEH-UHFFFAOYSA-N 1-phenyl-9h-fluoren-2-amine Chemical compound NC1=CC=C2C3=CC=CC=C3CC2=C1C1=CC=CC=C1 FPRFOKKPDUHQEH-UHFFFAOYSA-N 0.000 claims abstract description 6
- 239000000203 mixture Substances 0.000 claims description 51
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 claims description 46
- 239000004593 Epoxy Substances 0.000 claims description 45
- -1 aminophenyl Chemical group 0.000 claims description 26
- PXKLMJQFEQBVLD-UHFFFAOYSA-N bisphenol F Chemical compound C1=CC(O)=CC=C1CC1=CC=C(O)C=C1 PXKLMJQFEQBVLD-UHFFFAOYSA-N 0.000 claims description 16
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 claims description 16
- 125000003118 aryl group Chemical group 0.000 claims description 14
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 229920001187 thermosetting polymer Polymers 0.000 claims description 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 150000002367 halogens Chemical class 0.000 claims description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- 125000001931 aliphatic group Chemical group 0.000 claims description 4
- 230000001588 bifunctional effect Effects 0.000 claims description 4
- 150000002118 epoxides Chemical group 0.000 claims description 4
- 125000000524 functional group Chemical group 0.000 claims description 4
- 150000002431 hydrogen Chemical class 0.000 claims description 4
- 229920003986 novolac Polymers 0.000 claims description 4
- CIZUMWWHWPJAAK-UHFFFAOYSA-N 4-[9-(4-amino-3-chlorophenyl)fluoren-9-yl]-2-chloroaniline Chemical compound C1=C(Cl)C(N)=CC=C1C1(C=2C=C(Cl)C(N)=CC=2)C2=CC=CC=C2C2=CC=CC=C21 CIZUMWWHWPJAAK-UHFFFAOYSA-N 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
- UKJLNMAFNRKWGR-UHFFFAOYSA-N cyclohexatrienamine Chemical group NC1=CC=C=C[CH]1 UKJLNMAFNRKWGR-UHFFFAOYSA-N 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 239000000463 material Substances 0.000 claims description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 claims description 2
- SEFYJVFBMNOLBK-UHFFFAOYSA-N 2-[2-[2-(oxiran-2-ylmethoxy)ethoxy]ethoxymethyl]oxirane Chemical class C1OC1COCCOCCOCC1CO1 SEFYJVFBMNOLBK-UHFFFAOYSA-N 0.000 claims description 2
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 claims description 2
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 claims description 2
- KIFDSGGWDIVQGN-UHFFFAOYSA-N 4-[9-(4-aminophenyl)fluoren-9-yl]aniline Chemical compound C1=CC(N)=CC=C1C1(C=2C=CC(N)=CC=2)C2=CC=CC=C2C2=CC=CC=C21 KIFDSGGWDIVQGN-UHFFFAOYSA-N 0.000 claims description 2
- 150000001336 alkenes Chemical class 0.000 claims description 2
- 150000001408 amides Chemical class 0.000 claims description 2
- 229940106691 bisphenol a Drugs 0.000 claims description 2
- 229930003836 cresol Natural products 0.000 claims description 2
- 239000004643 cyanate ester Substances 0.000 claims 2
- 229920001567 vinyl ester resin Polymers 0.000 claims 2
- XQUPVDVFXZDTLT-UHFFFAOYSA-N 1-[4-[[4-(2,5-dioxopyrrol-1-yl)phenyl]methyl]phenyl]pyrrole-2,5-dione Chemical compound O=C1C=CC(=O)N1C(C=C1)=CC=C1CC1=CC=C(N2C(C=CC2=O)=O)C=C1 XQUPVDVFXZDTLT-UHFFFAOYSA-N 0.000 claims 1
- XFCUDCRKNNHSIW-UHFFFAOYSA-N 1-[9,9-bis(4-aminophenyl)fluoren-2-yl]ethanone Chemical compound C12=CC(C(=O)C)=CC=C2C2=CC=CC=C2C1(C=1C=CC(N)=CC=1)C1=CC=C(N)C=C1 XFCUDCRKNNHSIW-UHFFFAOYSA-N 0.000 claims 1
- CMLFRMDBDNHMRA-UHFFFAOYSA-N 2h-1,2-benzoxazine Chemical compound C1=CC=C2C=CNOC2=C1 CMLFRMDBDNHMRA-UHFFFAOYSA-N 0.000 claims 1
- RLJFPYAQWNGEGN-UHFFFAOYSA-N 4-[2-tert-butyl-9-[4-(methylamino)phenyl]fluoren-9-yl]-n-methylaniline Chemical compound C1=CC(NC)=CC=C1C1(C=2C=CC(NC)=CC=2)C2=CC(C(C)(C)C)=CC=C2C2=CC=CC=C21 RLJFPYAQWNGEGN-UHFFFAOYSA-N 0.000 claims 1
- FUBVPFZRLXXYJG-UHFFFAOYSA-N 4-[9-(4-amino-3,5-dichlorophenyl)fluoren-9-yl]-2,6-dichloroaniline Chemical compound C1=C(Cl)C(N)=C(Cl)C=C1C1(C=2C=C(Cl)C(N)=C(Cl)C=2)C2=CC=CC=C2C2=CC=CC=C21 FUBVPFZRLXXYJG-UHFFFAOYSA-N 0.000 claims 1
- UMAXFCDSAXELAT-UHFFFAOYSA-N 4-[9-(4-amino-3,5-diethylphenyl)fluoren-9-yl]-2,6-diethylaniline Chemical compound CCC1=C(N)C(CC)=CC(C2(C3=CC=CC=C3C3=CC=CC=C32)C=2C=C(CC)C(N)=C(CC)C=2)=C1 UMAXFCDSAXELAT-UHFFFAOYSA-N 0.000 claims 1
- LRQNMTUEZUJDMA-UHFFFAOYSA-N 4-[9-(4-amino-3,5-dimethylphenyl)fluoren-9-yl]-2,6-dimethylaniline Chemical compound CC1=C(N)C(C)=CC(C2(C3=CC=CC=C3C3=CC=CC=C32)C=2C=C(C)C(N)=C(C)C=2)=C1 LRQNMTUEZUJDMA-UHFFFAOYSA-N 0.000 claims 1
- KDYWXMLVTFANGF-UHFFFAOYSA-N 4-[9-(4-amino-3-ethylphenyl)fluoren-9-yl]-2-ethylaniline Chemical compound C1=C(N)C(CC)=CC(C2(C3=CC=CC=C3C3=CC=CC=C32)C=2C=C(CC)C(N)=CC=2)=C1 KDYWXMLVTFANGF-UHFFFAOYSA-N 0.000 claims 1
- VASAPMVFYCWJAC-UHFFFAOYSA-N 4-[9-(4-amino-3-methylphenyl)fluoren-9-yl]-2,6-diethylaniline Chemical compound CCC1=C(N)C(CC)=CC(C2(C3=CC=CC=C3C3=CC=CC=C32)C=2C=C(C)C(N)=CC=2)=C1 VASAPMVFYCWJAC-UHFFFAOYSA-N 0.000 claims 1
- YRKVLGUIGNRYJX-UHFFFAOYSA-N 4-[9-(4-amino-3-methylphenyl)fluoren-9-yl]-2-methylaniline Chemical group C1=C(N)C(C)=CC(C2(C3=CC=CC=C3C3=CC=CC=C32)C=2C=C(C)C(N)=CC=2)=C1 YRKVLGUIGNRYJX-UHFFFAOYSA-N 0.000 claims 1
- IWRAVODFRBEXME-UHFFFAOYSA-N 4-[9-(4-aminophenyl)-1-chlorofluoren-9-yl]aniline Chemical compound C1=CC(N)=CC=C1C1(C=2C=CC(N)=CC=2)C2=C(Cl)C=CC=C2C2=CC=CC=C21 IWRAVODFRBEXME-UHFFFAOYSA-N 0.000 claims 1
- YIIYKJRTZIJAJW-UHFFFAOYSA-N 4-[9-(4-aminophenyl)-2,6-dimethylfluoren-9-yl]aniline Chemical compound C=1C(C)=CC=C2C=1C1=CC=C(C)C=C1C2(C=1C=CC(N)=CC=1)C1=CC=C(N)C=C1 YIIYKJRTZIJAJW-UHFFFAOYSA-N 0.000 claims 1
- QGRDPVZBEAGAQT-UHFFFAOYSA-N 4-[9-(4-aminophenyl)-2,7-dichlorofluoren-9-yl]aniline Chemical compound C1=CC(N)=CC=C1C1(C=2C=CC(N)=CC=2)C2=CC(Cl)=CC=C2C2=CC=C(Cl)C=C21 QGRDPVZBEAGAQT-UHFFFAOYSA-N 0.000 claims 1
- AMRHANGJBYPGKE-UHFFFAOYSA-N 4-[9-(4-aminophenyl)-2,7-dinitrofluoren-9-yl]aniline Chemical compound C1=CC(N)=CC=C1C1(C=2C=CC(N)=CC=2)C2=CC([N+]([O-])=O)=CC=C2C2=CC=C([N+]([O-])=O)C=C21 AMRHANGJBYPGKE-UHFFFAOYSA-N 0.000 claims 1
- UTJKHWKMYHOCCL-UHFFFAOYSA-N 4-[9-(4-aminophenyl)-2-chloro-4-methylfluoren-9-yl]aniline Chemical compound CC1=CC(Cl)=CC2=C1C1=CC=CC=C1C2(C=1C=CC(N)=CC=1)C1=CC=C(N)C=C1 UTJKHWKMYHOCCL-UHFFFAOYSA-N 0.000 claims 1
- PBZLWMSBVHQLHN-UHFFFAOYSA-N 4-[9-(4-aminophenyl)-2-ethylfluoren-9-yl]aniline Chemical compound C12=CC(CC)=CC=C2C2=CC=CC=C2C1(C=1C=CC(N)=CC=1)C1=CC=C(N)C=C1 PBZLWMSBVHQLHN-UHFFFAOYSA-N 0.000 claims 1
- JOISDWWDEXYHCG-UHFFFAOYSA-N 4-[9-(4-aminophenyl)-2-fluorofluoren-9-yl]aniline Chemical compound C1=CC(N)=CC=C1C1(C=2C=CC(N)=CC=2)C2=CC(F)=CC=C2C2=CC=CC=C21 JOISDWWDEXYHCG-UHFFFAOYSA-N 0.000 claims 1
- WVVQDBOCZCWJRL-UHFFFAOYSA-N 4-[9-(4-aminophenyl)-2-iodofluoren-9-yl]aniline Chemical compound C1=CC(N)=CC=C1C1(C=2C=CC(N)=CC=2)C2=CC(I)=CC=C2C2=CC=CC=C21 WVVQDBOCZCWJRL-UHFFFAOYSA-N 0.000 claims 1
- YBZCMTYEYWQLNQ-UHFFFAOYSA-N 4-[9-(4-aminophenyl)-2-methylfluoren-9-yl]aniline Chemical compound C12=CC(C)=CC=C2C2=CC=CC=C2C1(C=1C=CC(N)=CC=1)C1=CC=C(N)C=C1 YBZCMTYEYWQLNQ-UHFFFAOYSA-N 0.000 claims 1
- XLCCSOUCJJGGKM-UHFFFAOYSA-N 4-[9-(4-aminophenyl)-3-bromofluoren-9-yl]aniline Chemical compound C1=CC(N)=CC=C1C1(C=2C=CC(N)=CC=2)C2=CC=C(Br)C=C2C2=CC=CC=C21 XLCCSOUCJJGGKM-UHFFFAOYSA-N 0.000 claims 1
- PHXKKHVBLDSVKR-UHFFFAOYSA-N 4-[9-(4-aminophenyl)-4-chlorofluoren-9-yl]aniline Chemical compound C1=CC(N)=CC=C1C1(C=2C=CC(N)=CC=2)C(C=CC=C2Cl)=C2C2=CC=CC=C21 PHXKKHVBLDSVKR-UHFFFAOYSA-N 0.000 claims 1
- PJBLZPUJWNTDPL-UHFFFAOYSA-N 4-[9-(4-aminophenyl)-4-methylfluoren-9-yl]aniline Chemical compound CC1=CC=CC2=C1C1=CC=CC=C1C2(C=1C=CC(N)=CC=1)C1=CC=C(N)C=C1 PJBLZPUJWNTDPL-UHFFFAOYSA-N 0.000 claims 1
- NQFKKMIEVCTUQS-UHFFFAOYSA-N 4-[9-[3,5-dimethyl-4-(methylamino)phenyl]-1,5-dimethylfluoren-9-yl]-n,2,6-trimethylaniline Chemical compound C1=C(C)C(NC)=C(C)C=C1C1(C=2C=C(C)C(NC)=C(C)C=2)C2=C(C)C=CC=C2C2=C(C)C=CC=C21 NQFKKMIEVCTUQS-UHFFFAOYSA-N 0.000 claims 1
- QFWYKFPCIFDQHB-UHFFFAOYSA-N 4-[9-[3,5-dimethyl-4-(methylamino)phenyl]fluoren-9-yl]-n,2,6-trimethylaniline Chemical compound C1=C(C)C(NC)=C(C)C=C1C1(C=2C=C(C)C(NC)=C(C)C=2)C2=CC=CC=C2C2=CC=CC=C21 QFWYKFPCIFDQHB-UHFFFAOYSA-N 0.000 claims 1
- WRIQVHHYPAKIFD-UHFFFAOYSA-N 4-[9-[4-(ethylamino)phenyl]fluoren-9-yl]-n-methylaniline Chemical compound C1=CC(NCC)=CC=C1C1(C=2C=CC(NC)=CC=2)C2=CC=CC=C2C2=CC=CC=C21 WRIQVHHYPAKIFD-UHFFFAOYSA-N 0.000 claims 1
- GWGFEVQYRQHGPQ-UHFFFAOYSA-N 4-[9-[4-(ethylamino)phenyl]fluoren-9-yl]aniline Chemical compound C1=CC(NCC)=CC=C1C1(C=2C=CC(N)=CC=2)C2=CC=CC=C2C2=CC=CC=C21 GWGFEVQYRQHGPQ-UHFFFAOYSA-N 0.000 claims 1
- TVOCKKPUJBBZLF-UHFFFAOYSA-N 4-[9-[4-(methylamino)phenyl]fluoren-9-yl]aniline Chemical compound C1=CC(NC)=CC=C1C1(C=2C=CC(N)=CC=2)C2=CC=CC=C2C2=CC=CC=C21 TVOCKKPUJBBZLF-UHFFFAOYSA-N 0.000 claims 1
- ZTSIAGQURKMHDL-UHFFFAOYSA-N C(C)NC1=CC=C(C=C1)C1=CC=CC=2C3=CC=CC=C3CC1=2 Chemical compound C(C)NC1=CC=C(C=C1)C1=CC=CC=2C3=CC=CC=C3CC1=2 ZTSIAGQURKMHDL-UHFFFAOYSA-N 0.000 claims 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims 1
- ZZTCPWRAHWXWCH-UHFFFAOYSA-N diphenylmethanediamine Chemical class C=1C=CC=CC=1C(N)(N)C1=CC=CC=C1 ZZTCPWRAHWXWCH-UHFFFAOYSA-N 0.000 claims 1
- 150000002170 ethers Chemical class 0.000 claims 1
- CDAQKWXLHGMZQP-UHFFFAOYSA-N n,2-dimethyl-4-[9-[3-methyl-4-(methylamino)phenyl]fluoren-9-yl]aniline Chemical compound C1=C(C)C(NC)=CC=C1C1(C=2C=C(C)C(NC)=CC=2)C2=CC=CC=C2C2=CC=CC=C21 CDAQKWXLHGMZQP-UHFFFAOYSA-N 0.000 claims 1
- DPNISTOAESHQJF-UHFFFAOYSA-N n-methyl-4-[2-methyl-9-[4-(methylamino)phenyl]fluoren-9-yl]aniline Chemical compound C1=CC(NC)=CC=C1C1(C=2C=CC(NC)=CC=2)C2=CC(C)=CC=C2C2=CC=CC=C21 DPNISTOAESHQJF-UHFFFAOYSA-N 0.000 claims 1
- WINGACDUUPIWFZ-UHFFFAOYSA-N n-methyl-4-[9-[4-(methylamino)phenyl]fluoren-9-yl]aniline Chemical group C1=CC(NC)=CC=C1C1(C=2C=CC(NC)=CC=2)C2=CC=CC=C2C2=CC=CC=C21 WINGACDUUPIWFZ-UHFFFAOYSA-N 0.000 claims 1
- JWFPOBHHFUZQOC-UHFFFAOYSA-N n-propyl-4-[9-[4-(propylamino)phenyl]fluoren-9-yl]aniline Chemical compound C1=CC(NCCC)=CC=C1C1(C=2C=CC(NCCC)=CC=2)C2=CC=CC=C2C2=CC=CC=C21 JWFPOBHHFUZQOC-UHFFFAOYSA-N 0.000 claims 1
- 239000005011 phenolic resin Substances 0.000 claims 1
- 229920003192 poly(bis maleimide) Polymers 0.000 claims 1
- 229920001225 polyester resin Polymers 0.000 claims 1
- 239000004645 polyester resin Substances 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 claims 1
- 239000012779 reinforcing material Substances 0.000 claims 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 229920006337 unsaturated polyester resin Polymers 0.000 claims 1
- 125000001624 naphthyl group Chemical group 0.000 description 26
- 125000003700 epoxy group Chemical group 0.000 description 15
- 239000000178 monomer Substances 0.000 description 15
- 230000009477 glass transition Effects 0.000 description 9
- 239000002243 precursor Substances 0.000 description 9
- 125000001424 substituent group Chemical group 0.000 description 7
- 150000001412 amines Chemical class 0.000 description 6
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 6
- 150000003141 primary amines Chemical class 0.000 description 6
- 125000003277 amino group Chemical group 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- NXPPAOGUKPJVDI-UHFFFAOYSA-N naphthalene-1,2-diol Chemical compound C1=CC=CC2=C(O)C(O)=CC=C21 NXPPAOGUKPJVDI-UHFFFAOYSA-N 0.000 description 5
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 4
- 125000002947 alkylene group Chemical group 0.000 description 4
- 239000003063 flame retardant Substances 0.000 description 4
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- FZZQNEVOYIYFPF-UHFFFAOYSA-N naphthalene-1,6-diol Chemical compound OC1=CC=CC2=CC(O)=CC=C21 FZZQNEVOYIYFPF-UHFFFAOYSA-N 0.000 description 4
- 229910052698 phosphorus Inorganic materials 0.000 description 4
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- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 3
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- 125000000467 secondary amino group Chemical class [H]N([*:1])[*:2] 0.000 description 3
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- AFEQENGXSMURHA-UHFFFAOYSA-N oxiran-2-ylmethanamine Chemical compound NCC1CO1 AFEQENGXSMURHA-UHFFFAOYSA-N 0.000 description 2
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 2
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- FRASJONUBLZVQX-UHFFFAOYSA-N 1,4-dioxonaphthalene Natural products C1=CC=C2C(=O)C=CC(=O)C2=C1 FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 description 1
- BOKGTLAJQHTOKE-UHFFFAOYSA-N 1,5-dihydroxynaphthalene Chemical compound C1=CC=C2C(O)=CC=CC2=C1O BOKGTLAJQHTOKE-UHFFFAOYSA-N 0.000 description 1
- ZPANWZBSGMDWON-UHFFFAOYSA-N 1-[(2-hydroxynaphthalen-1-yl)methyl]naphthalen-2-ol Chemical compound C1=CC=C2C(CC3=C4C=CC=CC4=CC=C3O)=C(O)C=CC2=C1 ZPANWZBSGMDWON-UHFFFAOYSA-N 0.000 description 1
- AECOSYUGANNAOK-UHFFFAOYSA-N 1-[(7-hydroxynaphthalen-1-yl)methyl]naphthalen-2-ol Chemical compound C1=CC=C2C(CC3=CC=CC4=CC=C(C=C43)O)=C(O)C=CC2=C1 AECOSYUGANNAOK-UHFFFAOYSA-N 0.000 description 1
- SDAYVSWWJWIHPP-UHFFFAOYSA-N 1-[methyl-(4-nitrophenoxy)phosphoryl]oxy-4-nitrobenzene Chemical compound C=1C=C([N+]([O-])=O)C=CC=1OP(=O)(C)OC1=CC=C([N+]([O-])=O)C=C1 SDAYVSWWJWIHPP-UHFFFAOYSA-N 0.000 description 1
- MEVBAGCIOOTPLF-UHFFFAOYSA-N 2-[[5-(oxiran-2-ylmethoxy)naphthalen-2-yl]oxymethyl]oxirane Chemical compound C1OC1COC(C=C1C=CC=2)=CC=C1C=2OCC1CO1 MEVBAGCIOOTPLF-UHFFFAOYSA-N 0.000 description 1
- BZVQIZYWIWXTHX-UHFFFAOYSA-N 2-[[methyl(oxiran-2-ylmethoxy)phosphoryl]oxymethyl]oxirane Chemical compound C1OC1COP(=O)(C)OCC1CO1 BZVQIZYWIWXTHX-UHFFFAOYSA-N 0.000 description 1
- KQCDNTFMEXGZKZ-UHFFFAOYSA-N 2-[[oxiran-2-ylmethoxy(phenyl)phosphoryl]oxymethyl]oxirane Chemical compound C1OC1COP(C=1C=CC=CC=1)(=O)OCC1CO1 KQCDNTFMEXGZKZ-UHFFFAOYSA-N 0.000 description 1
- YBRVSVVVWCFQMG-UHFFFAOYSA-N 4,4'-diaminodiphenylmethane Chemical class C1=CC(N)=CC=C1CC1=CC=C(N)C=C1 YBRVSVVVWCFQMG-UHFFFAOYSA-N 0.000 description 1
- FYZNZNUQAVALHR-UHFFFAOYSA-N 4-[(4-aminophenoxy)-methylphosphoryl]oxyaniline Chemical compound C=1C=C(N)C=CC=1OP(=O)(C)OC1=CC=C(N)C=C1 FYZNZNUQAVALHR-UHFFFAOYSA-N 0.000 description 1
- FVCSARBUZVPSQF-UHFFFAOYSA-N 5-(2,4-dioxooxolan-3-yl)-7-methyl-3a,4,5,7a-tetrahydro-2-benzofuran-1,3-dione Chemical compound C1C(C(OC2=O)=O)C2C(C)=CC1C1C(=O)COC1=O FVCSARBUZVPSQF-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000002723 alicyclic group Chemical group 0.000 description 1
- 239000004844 aliphatic epoxy resin Substances 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000005600 alkyl phosphonate group Chemical group 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- 229920003180 amino resin Polymers 0.000 description 1
- 239000004760 aramid Substances 0.000 description 1
- 229920003235 aromatic polyamide Polymers 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000002102 aryl alkyloxo group Chemical group 0.000 description 1
- 125000004104 aryloxy group Chemical group 0.000 description 1
- IWZNWGDJJJKIOC-UHFFFAOYSA-N bis(3-aminophenyl)methyl-oxidophosphanium Chemical compound NC=1C=C(C=CC1)C(C1=CC(=CC=C1)N)[PH2]=O IWZNWGDJJJKIOC-UHFFFAOYSA-N 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 230000001143 conditioned effect Effects 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 239000011353 cycloaliphatic epoxy resin Substances 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000003631 expected effect Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 125000001475 halogen functional group Chemical group 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000003754 machining Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- HXZSFRJGDPGVNY-UHFFFAOYSA-N methyl(oxido)phosphanium Chemical compound C[PH2]=O HXZSFRJGDPGVNY-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- PYNVYLAZKQQFLK-UHFFFAOYSA-N naphthalene-1,2,3,4-tetrol Chemical compound C1=CC=CC2=C(O)C(O)=C(O)C(O)=C21 PYNVYLAZKQQFLK-UHFFFAOYSA-N 0.000 description 1
- NCIAGQNZQHYKGR-UHFFFAOYSA-N naphthalene-1,2,3-triol Chemical compound C1=CC=C2C(O)=C(O)C(O)=CC2=C1 NCIAGQNZQHYKGR-UHFFFAOYSA-N 0.000 description 1
- XOOMNEFVDUTJPP-UHFFFAOYSA-N naphthalene-1,3-diol Chemical compound C1=CC=CC2=CC(O)=CC(O)=C21 XOOMNEFVDUTJPP-UHFFFAOYSA-N 0.000 description 1
- PCILLCXFKWDRMK-UHFFFAOYSA-N naphthalene-1,4-diol Chemical compound C1=CC=C2C(O)=CC=C(O)C2=C1 PCILLCXFKWDRMK-UHFFFAOYSA-N 0.000 description 1
- ZUVBIBLYOCVYJU-UHFFFAOYSA-N naphthalene-1,7-diol Chemical compound C1=CC=C(O)C2=CC(O)=CC=C21 ZUVBIBLYOCVYJU-UHFFFAOYSA-N 0.000 description 1
- JRNGUTKWMSBIBF-UHFFFAOYSA-N naphthalene-2,3-diol Chemical compound C1=CC=C2C=C(O)C(O)=CC2=C1 JRNGUTKWMSBIBF-UHFFFAOYSA-N 0.000 description 1
- DFQICHCWIIJABH-UHFFFAOYSA-N naphthalene-2,7-diol Chemical compound C1=CC(O)=CC2=CC(O)=CC=C21 DFQICHCWIIJABH-UHFFFAOYSA-N 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 125000000466 oxiranyl group Chemical group 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 238000005502 peroxidation Methods 0.000 description 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- BCMKHWMDTMUUSI-UHFFFAOYSA-N tetrahydroxynaphthalene Natural products OC1=CC(O)=CC2=CC(O)=CC(O)=C21 BCMKHWMDTMUUSI-UHFFFAOYSA-N 0.000 description 1
- PYGKDFLMCGZPHX-UHFFFAOYSA-N tris(oxiran-2-ylmethyl) phosphate Chemical compound C1OC1COP(OCC1OC1)(=O)OCC1CO1 PYGKDFLMCGZPHX-UHFFFAOYSA-N 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
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- C08G59/24—Di-epoxy compounds carbocyclic
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- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
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- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
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Abstract
Description
−ASTM D5045−99(2007)e1に従って測定して、500から1000J/m2、好ましくは700から1000J/m2の範囲、及び/又は前述の範囲の組合せの臨界ひずみエネルギー解放率G1c;
−ASTM D5045−99(2007)e1に従って測定して、1.0から2.5MPa0.5、好ましくは1.4から2.0MPa0.5若しくは1.6から2.0MPa0.5の範囲、及び/又は前述の範囲の組合せの臨界応力拡大係数K1c;
−ASTM D790に従って測定して、3.0から3.8の範囲、好ましくは3.2から3.6、若しくは3.0から3.8、若しくは3.3から3.5の範囲、及び/又は前述の範囲の組合せの弾性率G;
−Tg開始(乾燥)は、130から220℃、若しくは150から200℃、若しくは好ましくは170℃から190℃の範囲、及び/又は前述の範囲の組合せである;
−Tg開始(湿潤)は、100から180℃、若しくは120から170℃、好ましくは130℃から160℃、若しくは125から145℃の範囲、及び/又は前述の範囲の組合せである;
を有し、各R0は、水素、並びにエポキシド基含有化合物を重合する際に不活性な基(好ましくはハロゲン、1から6個の炭素原子を有する直鎖及び分岐アルキル基、フェニル、ニトロ、アセチル及びトリメチルシリルから選択される)から独立して選択され;各Rは、水素、並びに1から6個の炭素原子を有する直鎖及び分岐アルキル基から独立して選択され;各R1は、R、水素、フェニル及びハロゲンから独立して選択される。
(式中、各R2は、水素、並びに1から6個の炭素原子を有する直鎖及び分岐アルキル基から独立して選択され、少なくともR2の25モル%は直鎖又は分岐アルキルであり、各R3は、水素、1から6個の炭素原子を有する直鎖及び分岐アルキル基、フェニル、ハロゲンから独立して選択され、各R0は、式Iに定義されている通りである)を有する9,9−ビス(アミノフェニル)フルオレンによって得られ、(b)エポキシ樹脂硬化剤の80から0モル%は、好ましくは、脂肪族ポリアミン、芳香族ポリアミン、芳香族ポリアミド、脂環式ポリアミン、ポリアミン、ポリアミド及びアミノ樹脂から選択される。最も好ましくは、エポキシ樹脂硬化剤は、9,9−ビス(4−アミノフェニル)フルオレン、例えば9,9−ビス(4アミノ−3−クロロ−フェニル(フルオレン))である。
KaneAceにより供給されている、コアシェルゴム組成物MX136を用意した。この組成物は、220エポキシ当量(EEW)のビスフェノールFエポキシ樹脂及びコアシェルゴム粒子の25重量%の分散系を含有する。
例1と同一のプロセスを使用すると、樹脂は同一の成分から調製されるが、さらに、Huntsmanから供給された、ナフタレンエポキシ樹脂MY816(1.6ジヒドロキシナフタレンのジグリシジルエーテル)を以下に示す量の樹脂配合物に様々な量で加えた:
Claims (18)
- 複合部品を作製するための樹脂組成物であって、
a.グリシジルエーテルエポキシ樹脂を含む第1の樹脂成分、
b.ナフタレン系エポキシ樹脂を含む第2の樹脂成分、
c.アミノフェニルフルオレン硬化剤
を含み、エポキシ樹脂成分a)及びb)が、33重量%までの第2の樹脂成分を含有する、上記樹脂組成物。 - 190℃で120分間硬化させた場合、少なくとも130℃の湿潤Tgを有する、請求項1に記載の組成物。
- 前記硬化剤が、構造式
を有し、各R0が、水素、及び、エポキシド基含有化合物を重合する際に不活性な基(好ましくはハロゲン、1から6個の炭素原子を有する直鎖及び分岐アルキル基、フェニル、ニトロ、アセチル及びトリメチルシリルから選択される)から独立して選択され;
各Rが、水素、並びに1から6個の炭素原子を有する直鎖及び分岐アルキル基から独立して選択され;
各R1が、R、水素、フェニル及びハロゲンから独立して選択される、
請求項1又は2に記載の組成物。 - 前記硬化剤が、以下の硬化剤:9,9−ビス(4−アミノフェニル)フルオレン、4−メチル−9,9−ビス(4−アミノフェニル)フルオレン、4−クロロ−9,9−ビス(4−アミノフェニル)フルオレン、2−エチル−9,9−ビス(4−アミノフェニル)フルオレン、2−ヨード−9,9−ビス(4−アミノフェニル)フルオレン、3−ブロモ−9,9−ビス(4−アミノフェニル)フルオレン、9−(4−メチルアミノフェニル)−9−(4−エチルアミノフェニル)フルオレン、1−クロロ−9,9−ビス(4−アミノフェニル)フルオレン、2−メチル−9,9−ビス(4−アミノフェニル)フルオレン、2,6−ジメチル−9,9−ビス(4−アミノフェニル)フルオレン、1,5−ジメチル−9,9−ビス(4−アミノフェニル)フルオレン、2−フルオロ−9,9−ビス(4−アミノフェニル)フルオレン、1,2,3,4,5,6,7,8−オクタフルオロ−9,9−ビス(4−アミノフェニル)フルオレン、2,7−ジニトロ−9,9−ビス(4−アミノフェニル)フルオレン、2−クロロ−4−メチル−9,9−ビス(4−アミノフェニル)フルオレン、2,7−ジクロロ−9,9−ビス(4−アミノフェニル)フルオレン、2−アセチル−9,9−ビス(4−アミノフェニル)フルオレン、2−メチル−9,9−ビス(4−メチルアミノフェニル)フルオレン、2−クロロ−9,9−ビス(4−エチルアミノフェニル)フルオレン、又は2−t−ブチル−9,9−ビス(4−メチルアミノフェニル)フルオレンの1つ又は複数を含む、請求項1から3までのいずれか一項に記載の組成物。
- 前記硬化剤が、以下の硬化剤:ビス(二級アミノフェニル)フルオレン、又はビス(二級アミノフェニル)フルオレン及び(一級アミノフェニル)(二級アミノフェニル)フルオレンの混合物の1つ又は複数を含む、請求項1から4までのいずれか一項に記載の組成物。
- 前記硬化剤が、9,9−ビス(4−メチルアミノフェニル)フルオレン、9−(4−メチルアミノフェニル)−9−(4−アミノフェニル)フルオレン、9,9−ビス(4−エチルアミノフェニル)フルオレン、9−(4−エチルアミノフェニル)−9−(4−アミノフェニル)フルオレン、9,9−ビス(4−プロピルアミノフェニル)フルオレン、9,9−ビス(4−イソプロピルアミノフェニル)フルオレン、9,9−ビス(4−ブチルアミノフェニル)フルオレン、9,9−ビス(3−メチル−4−メチルアミノフェニル)フルオレン、9,9−ビス(3−クロロ−4−メチルアミノフェニル)フルオレン、9−(4−メチルアミノフェニル)−9−(4−エチルアミノフェニル)フルオレン、4−メチル−9,9−ビス(4−メチルアミノフェニル)フルオレン又は4−クロロ−9,9−ビス(4−メチルアミノフェニル)フルオレンを含む、請求項5に記載の組成物。
- 前記硬化剤が、立体障害されたビス(一級アミノフェニル)フルオレンを含む、請求項5に記載の組成物。
- 前記硬化剤が、9,9−ビス(3−メチル−4−アミノフェニル)フルオレン、9,9−ビス(3−エチル−4−アミノフェニル)フルオレン、9,9−ビス(3−フェニル−4−アミノフェニル)フルオレン、9,9−ビス(3,5−ジメチル−4−メチルアミノフェニル)フルオレン、9,9−ビス(3,5−ジメチル−4−アミノフェニル)フルオレン、9−(3,5−ジメチル−4−メチルアミノフェニル)−9−(3,5−ジメチル−4−アミノフェニル)フルオレン、9−(3,5−ジエチル−4−アミノフェニル)−9−(3−メチル−4−アミノフェニル)フルオレン、1,5−ジメチル−9,9−ビス(3,5−ジメチル−4−メチルアミノフェニル)フルオレン、9,9−ビス(3,5−ジイソプロピル−4−アミノフェニル)フルオレン、9,9−ビス(3−クロロ−4−アミノフェニル)フルオレン、9,9−ビス(3,5−ジクロロ−4−アミノフェニル)フルオレン、9,9−ビス(3,5−ジエチル−4−メチルアミノフェニル)フルオレン又は9,9−ビス(3,5−ジエチル−4−アミノフェニル)フルオレンを含む、請求項5に記載の組成物。
- 前記硬化剤が、ハロゲン置換されたアミノフェニルフルオレン硬化剤を含む、請求項1から8までのいずれか一項に記載の組成物。
- 前記第2の樹脂成分が、ビスフェノール−A(BPA)ジグリシジルエーテル及び/又はビスフェノール−F(BPF)ジグリシジルエーテル並びにそれらの誘導体の少なくとも1つを含む、請求項1から9までのいずれか一項に記載の組成物。
- 第1の成分が、二官能性エポキシ樹脂を含み、好ましくは二官能性エポキシが、2個のエポキシ官能基を有する、請求項10に記載の組成物。
- 前記二官能性エポキシ樹脂が、ビスフェノールFのジグリシジルエーテル、(場合により臭素化された)ビスフェノールA、フェノール及びクレゾールエポキシノボラック、フェノール−アルデリド付加体のグリシジルエーテル、脂肪族ジオールのグリシジルエーテル、ジグリシジルエーテル、ジエチレングリコールジグリシジルエーテル、芳香族エポキシ樹脂、脂肪族ポリグリシジルエーテル、エポキシ化オレフィン、臭素化樹脂、芳香族グリシジルアミン、複素環式グリシジルイミジン及びアミド、グリシジルエーテル、フッ素化エポキシ樹脂、及び/又は前述の樹脂の任意の組合せ
を含む請求項11に記載の組成物。 - 前記第2の成分が、10重量%以上の量で、好ましくは15重量%以上の量で、より好ましくは20重量%以上の量で存在する、請求項1から12までのいずれか一項に記載の組成物。
- 前記組成物の非ナフタレン成分が、90重量%以下の量で、好ましくは85重量%以下の量で、より好ましくは80重量%以下の量で存在する、請求項1から13までのいずれか一項に記載の組成物。
- 前記組成物が、別の熱硬化性樹脂も含み、該別の熱硬化性樹脂が、本明細書に記載されているナフタレン系エポキシ樹脂でも、非ナフタレンエポキシ樹脂でもない、請求項1から14までのいずれか一項に記載の組成物。
- 少なくとも1つの別の熱硬化性樹脂も含む、請求項1から15までのいずれか一項に記載の組成物。
- 前記別の熱硬化性樹脂が、シアン酸エステル樹脂、ビニルエステル樹脂、ベンゾオキサジン樹脂、ビスマレイミド樹脂、ビニルエステル樹脂、フェノール樹脂、ポリエステル樹脂、不飽和ポリエステル樹脂、シアン酸エステル樹脂、4,4’−ジアミノジフェニルメタン(TGDDM)のテトラグリシジル誘導体、アミノフェノール(TGAP)のトリグリシジル誘導体、エポキシノボラック及びその誘導体、並びに/又は前述の樹脂の任意の組合せから選択される、請求項16に記載の組成物。
- 樹脂材料及び強化材料を含む、複合部品を作製するための樹脂系の使用であって、該樹脂系が、該樹脂材料の少なくとも一部を形成し、前記系が、
エポキシ樹脂成分、
アミノフェニルフルオレン硬化剤
を含み、エポキシ樹脂成分の33重量%までが、1つ又は複数のナフタレン系エポキシ樹脂成分を構成する、
上記使用。
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CA2880428A1 (en) | 2014-04-03 |
WO2014049028A2 (en) | 2014-04-03 |
CN104684955A (zh) | 2015-06-03 |
RU2015115718A (ru) | 2016-11-20 |
US9695312B2 (en) | 2017-07-04 |
RU2647850C2 (ru) | 2018-03-21 |
WO2014049028A3 (en) | 2014-05-22 |
ES2792901T3 (es) | 2020-11-12 |
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